Dipartimento di Scienze Chimiche, Università di Padova, via Marzolo 1, Padova, I-35131, Italy.
Dipartimento di Scienze Biomediche, Università di Padova, via U. Bassi 58/B1, Padova, I-35131, Italy.
Biomacromolecules. 2021 Feb 8;22(2):467-480. doi: 10.1021/acs.biomac.0c01321. Epub 2020 Dec 21.
Herein we present an innovative approach to produce biocompatible, degradable, and stealth polymeric nanoparticles based on poly(lipoic acid), stabilized by a PEG-ended surfactant. Taking advantage of the well-known thiol-induced polymerization of lipoic acid, a universal and nontoxic nanovector consisted of a solid cross-linked polymeric matrix of lipoic acid monomers was prepared and loaded with active species with a one-step protocol. The biological studies demonstrated a high stability in biological media, the virtual absence of "protein" corona in biological fluids, the absence of acute toxicity in vitro and in vivo, complete clearance from the organism, and a relevant preference for short-term accumulation in the heart. All these features make these nanoparticles candidates as a promising tool for nanomedicine.
在这里,我们提出了一种生产基于聚(硫辛酸)的生物相容、可降解和隐形聚合物纳米粒子的创新方法,该聚合物纳米粒子由 PEG 端接的表面活性剂稳定。利用众所周知的硫醇诱导的硫辛酸聚合,制备了由硫辛酸单体的交联聚合物基质组成的通用且无毒的纳米载体,并通过一步法负载活性物质。生物学研究表明,该纳米载体在生物介质中具有高稳定性,在生物流体中几乎不存在“蛋白质”冠,体外和体内无急性毒性,能完全从体内清除,并在心脏中有明显的短期积累倾向。所有这些特性使这些纳米粒子成为纳米医学的一种有前途的工具。